Author/Creator: Tepeli, Emre - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Tepeli, Emre

1. A variant allele of the Mediterranean‐fever gene increases the severity of gout. (29th April 2016)

Authors:: Balkarli, Ayse; Tepeli, Emre; Balkarli, Huseyin; Kaya, Arif; Cobankara, Veli
Journal:: International journal of rheumatic diseases
Issue:: Volume 21:Number 1(2018)
Page Start:: 338
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder. (August 2019)

Authors:: Aydin, Sezai Ustun; Kabukcu Basay, Burge; Cetin, Gokhan Ozan; Gungor Aydin, Aysegul; Tepeli, Emre
Journal:: Journal of psychiatric research
Issue:: Volume 115(2019)
Page Start:: 158
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age‐related macular degeneration?. (19th August 2014)

Authors:: Okur, Volkan; Cetin, Ozan; Cetin, Ebru; Tepeli, Emre; Bulgu, Yunus; Yildirim, Cem
Journal:: Clinical & experimental ophthalmology
Issue:: Volume 43:Number 1(2015)
Page Start:: 47
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Interleukin-1 gene (IL-1) polymorphism in patients with Behçet's Disease, and its relationship with disease manifestations. (21st July 2022)

Authors:: Özkan, Ümit; Ulutaş, Firdevs; Tepeli, Emre; Çobankara, Veli
Journal:: European journal of inflammation
Issue:: Volume 20(2022)
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

5. Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association. Issue 9 (29th September 2016)

Authors:: Özdemir, Özmert MA; Çıralı, Ceren; Yılmaz Ağladıoğlu, Sebahat; Evrengül, Havva; Tepeli, Emre; Ergin, Hacer
Journal:: Pediatrics international
Issue:: Volume 58:Issue 9(2016)
Page Start:: 912
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

6. Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association. Issue 9 (September 2016)

Authors:: Özdemir, Özmert MA; Çıralı, Ceren; Yılmaz Ağladıoğlu, Sebahat; Evrengül, Havva; Tepeli, Emre; Ergin, Hacer
Journal:: Pediatrics international
Issue:: Volume 58:Issue 9(2016)
Page Start:: 912
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗